| From: | beemanne@york.uchsc.edu (Neal Beeman) (by way of histonet) |
| To: | histonet <histonet@magicnet.net> |
| Reply-To: | |
| Content-Type: | text/plain; charset="us-ascii" |
I want to stain nuclei in frozen sections with neutral red. Does anyone have a handy protocol? Also, the protocol I have looked at calls for 0.1M acetate buffer at pH 3.0-5.5. Can I use Tris buffer instead? Neal